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Physical Activity Protects the Pathological Alterations of Alzheimer’s Disease Kidneys via the Activation of PACAP and BMP Signaling Pathways
Alzheimer’s disease (AD) is a neurodegenerative disorder with typical amyloid beta (Aβ) aggregations. Elimination of the Aβ precursors via the kidneys makes the organ a potential factor in the systemic degeneration leading to AD. Pituitary adenylate cyclase-activating polypeptide (PACAP) exerts neur...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7457084/ https://www.ncbi.nlm.nih.gov/pubmed/32922265 http://dx.doi.org/10.3389/fncel.2020.00243 |
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author | Perényi, Helga Szegeczki, Vince Horváth, Gabriella Hinnah, Barbara Tamás, Andrea Radák, Zsolt Ábrahám, Dóra Zákány, Róza Reglodi, Dora Juhász, Tamás |
author_facet | Perényi, Helga Szegeczki, Vince Horváth, Gabriella Hinnah, Barbara Tamás, Andrea Radák, Zsolt Ábrahám, Dóra Zákány, Róza Reglodi, Dora Juhász, Tamás |
author_sort | Perényi, Helga |
collection | PubMed |
description | Alzheimer’s disease (AD) is a neurodegenerative disorder with typical amyloid beta (Aβ) aggregations. Elimination of the Aβ precursors via the kidneys makes the organ a potential factor in the systemic degeneration leading to AD. Pituitary adenylate cyclase-activating polypeptide (PACAP) exerts neuroprotective effects in AD and plays a protective role in kidney pathologies. Increased physical activity is preventive of the formation of AD, but its detailed mechanism and possible connections with PACAP have not been clarified. In the kidneys of AD mice, the effects of physical activity were investigated by comparing wild-type and AD organs. Aβ plaque formation was reduced in AD kidneys after increased training (TAD). Mechanotransduction elevated PACAP receptor expression in TAD mice and normalized the protein kinase A (PKA)-mediated pathways. BMP4/BMPR1 elevation activated Smad1 expression and normalized collagen type IV in TAD animals. In conclusion, our data suggest that elevated physical activity can prevent the AD-induced pathological changes in the kidneys via, at least in part, the activation of PACAP–BMP signaling crosstalk. |
format | Online Article Text |
id | pubmed-7457084 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-74570842020-09-11 Physical Activity Protects the Pathological Alterations of Alzheimer’s Disease Kidneys via the Activation of PACAP and BMP Signaling Pathways Perényi, Helga Szegeczki, Vince Horváth, Gabriella Hinnah, Barbara Tamás, Andrea Radák, Zsolt Ábrahám, Dóra Zákány, Róza Reglodi, Dora Juhász, Tamás Front Cell Neurosci Neuroscience Alzheimer’s disease (AD) is a neurodegenerative disorder with typical amyloid beta (Aβ) aggregations. Elimination of the Aβ precursors via the kidneys makes the organ a potential factor in the systemic degeneration leading to AD. Pituitary adenylate cyclase-activating polypeptide (PACAP) exerts neuroprotective effects in AD and plays a protective role in kidney pathologies. Increased physical activity is preventive of the formation of AD, but its detailed mechanism and possible connections with PACAP have not been clarified. In the kidneys of AD mice, the effects of physical activity were investigated by comparing wild-type and AD organs. Aβ plaque formation was reduced in AD kidneys after increased training (TAD). Mechanotransduction elevated PACAP receptor expression in TAD mice and normalized the protein kinase A (PKA)-mediated pathways. BMP4/BMPR1 elevation activated Smad1 expression and normalized collagen type IV in TAD animals. In conclusion, our data suggest that elevated physical activity can prevent the AD-induced pathological changes in the kidneys via, at least in part, the activation of PACAP–BMP signaling crosstalk. Frontiers Media S.A. 2020-08-14 /pmc/articles/PMC7457084/ /pubmed/32922265 http://dx.doi.org/10.3389/fncel.2020.00243 Text en Copyright © 2020 Perényi, Szegeczki, Horváth, Hinnah, Tamás, Radák, Ábrahám, Zákány, Reglodi and Juhász. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Perényi, Helga Szegeczki, Vince Horváth, Gabriella Hinnah, Barbara Tamás, Andrea Radák, Zsolt Ábrahám, Dóra Zákány, Róza Reglodi, Dora Juhász, Tamás Physical Activity Protects the Pathological Alterations of Alzheimer’s Disease Kidneys via the Activation of PACAP and BMP Signaling Pathways |
title | Physical Activity Protects the Pathological Alterations of Alzheimer’s Disease Kidneys via the Activation of PACAP and BMP Signaling Pathways |
title_full | Physical Activity Protects the Pathological Alterations of Alzheimer’s Disease Kidneys via the Activation of PACAP and BMP Signaling Pathways |
title_fullStr | Physical Activity Protects the Pathological Alterations of Alzheimer’s Disease Kidneys via the Activation of PACAP and BMP Signaling Pathways |
title_full_unstemmed | Physical Activity Protects the Pathological Alterations of Alzheimer’s Disease Kidneys via the Activation of PACAP and BMP Signaling Pathways |
title_short | Physical Activity Protects the Pathological Alterations of Alzheimer’s Disease Kidneys via the Activation of PACAP and BMP Signaling Pathways |
title_sort | physical activity protects the pathological alterations of alzheimer’s disease kidneys via the activation of pacap and bmp signaling pathways |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7457084/ https://www.ncbi.nlm.nih.gov/pubmed/32922265 http://dx.doi.org/10.3389/fncel.2020.00243 |
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